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. 2018 Sep 26;10(10):356. doi: 10.3390/cancers10100356

Table 1.

Genetic modification of oncolytic viruses.

Virus Classification Oncolytic Virus Genetic Modification Manufacturer
Herpes Simplex Virus-1
(DNA Virus)
T-VEC
(talimogene laherparepvec, Imlygic®)
ICP34.5 deletion, ICP47 deletion, GMCSF insertion Amgen Inc., Thousand Oaks, USA
HF10
(canerpaturev—C-REV)
Natural deletion and insertion led to loss of expression of UL43, Ul49.5, UL55, UL56, and LAT Takara Bio Inc., Kusatsu, Shiga, Japan
HSV1716
(Seprehvir®)
ICP34.5 deletion Virttu Biologics, Glasgow, U.K.
G207 ICP34.5 deletion, ICP6 deletion, and LacZ insertion Medigene, Planegg, Germany
G47∆ ICP34.5 deletion, ICP6 deletion, ICP47 deletion, and LacZ insertion Daiichi Sankyo Company, Tokyo, Japan
M032 ICP34.5 deletion and IL12 insertion Aettis, Inc., Pennsylvania, USA
OrienX010 ICP34.5 and ICP47 deletion, and GM-CSF insertion Orien Gene Biotechnology, Zhejiang, China
Adenoviruses
(DNA Virus)
H101
(Oncorine)
E1B deletion and E3 partial deletion Shanghai Sunway Biotech, Shanghai, China
ONYX-015 E1B-55 KDa gene deletion Onyx pharmaceutical, South San Francisco, USA
ONCOS-102 (formerly named CGTG-102) adeno ∆24-RGD-GM-CSF insertion Targovax
(Merged with ONCOS therapeutic), Oslo, Norway
VCN-01 pRb-dependent; loaded with genes encoding PH20 hyaluronidase VCN Biosciences SL, Barcelona, Spain
LOAd-703 pRb-dependent; loaded with genes encoding CD40L and 4-1BBL Lokon Pharma, Uppsala, Sweden
ICOVIR-7 pRb-dependent adenovirus with 24-bp deletion in E1A. The fiber of the capsid has been modified with an RGD-4C motif in the HI-loop with a E2F promoter, and E1A deletion, the replication is optimized with E2F binding hairpins and contains Kozak sequence Targovax
(Merged with Oncos therapeutics), Oslo, Norway
ICOVIR-5 Adeno ∆24-RGD, pRb-dependent adenovirus, with a deletion in 24bp in EIA with E2F promoter and contains the Kozak sequence at the E1a start codon Institut Català d’Oncologia, Barcelona, Spain
DNX-2401 Deletion in 24bp in EIA and RGD-motif was engineered into the fiber H-loop, enabling the virus
to use αvβ3 or αvβ5 an integrins to enter cells
DNAtrix, Houston, USA
Vaccinia Viruses (DNA Virus) Pexastimogene devacirepvec
(PexaVec)
(formerly named JX-594)
Thymidine kinase deletion and GM-CSF insertion SillaJen, Busan, Korea
Reovirus
(RNA Virus)
Pelareorep (Reolysin®) Natural virus Oncolytics Biotech® Inc., Calgary, Canada
Paramyxoviridae Family Measles virus hNIS insertion for MV-NIS and Carcinoembryonic antigen (CEA) insertion for MV-CEA Vyriad, Rochester, USA
Newcastle disease virus (NDV) Natural virus Hadassah medical organization,
Parvovirus
(RNA Virus)
Parvovirus H-1 (ParvOryx) Natural virus ORYX Medicine, Vaterstetten, Germany
Picornaviruses
(RNA Virus)
CVA21 (Cavatak) Natural virus Viralytics, Sydney, Australia
PVSRIPO CD155/Necl5 dependent poliovirus. The internal ribosome entry site (IRES) of the poliovirus replaced with the IRES from human rhinovirus type 2 (HRV2) Duke University, Durham, USA
Retroviral Replicating Vectors TOCA51 This vector is based on murine leukemia virus (MLV) and carrying the yeast cytosine deaminase (CD) that convert 5-fluorocytosine (5-FC) into in the presence of CD, to 5-fluorouracil (5-FU). Tocagen, San Diego, USA

The table includes the oncolytic viruses that were mentioned in this review. GM-CSF—granulocyte-macrophage colony-stimulating factor.